Bello-Ortí Bernardo, Aragon Virginia, Pina-Pedrero Sonia, Bensaid Albert
Centre de Recerca en Sanitat Animal (CReSA), UAB-IRTA, Campus de la Universitat Autònoma de Barcelona, 08193 Bellaterra, Barcelona, Spain.
Institut de Recerca i Tecnologia Agroalimentàries (IRTA), Barcelona, Spain.
Microbiology (Reading). 2014 Sep;160(Pt 9):1974-1984. doi: 10.1099/mic.0.079483-0. Epub 2014 Jun 20.
Haemophilus parasuis is the causative agent of Glässer's disease, a systemic disorder characterized by polyarthritis, polyserositis and meningitis in pigs. Although it is well known that H. parasuis serovar 5 is the most prevalent serovar associated with the disease, the genetic differences among strains are only now being discovered. Genomes from two serovar 5 strains, SH0165 and 29755, are already available. Here, we present the draft genome of a third H. parasuis serovar 5 strain, the formal serovar 5 reference strain Nagasaki. An in silico genome subtractive analysis with full-length predicted genes of the three H. parasuis serovar 5 strains detected 95, 127 and 95 strain-specific genes (SSGs) for Nagasaki, SH0165 and 29755, respectively. We found that the genomic diversity within these three strains was high, in part because of a high number of mobile elements. Furthermore, a detailed analysis of large sequence polymorphisms (LSPs), encompassing regions ranging from 2 to 16 kb, revealed LSPs in virulence-related elements, such as a Toll-IL receptor, the AcrA multidrug efflux protein, an ATP-binding cassette (ABC) transporter, lipopolysaccharide-synthetizing enzymes and a tripartite ATP-independent periplasmic (TRAP) transporter. The whole-genome codon adaptation index (CAI) was also calculated and revealed values similar to other well-known bacterial pathogens. In addition, whole-genome SNP analysis indicated that nucleotide changes tended to be increased in membrane-related genes. This analysis provides further evidence that the genome of H. parasuis has been subjected to multiple lateral gene transfers (LGTs) and to fine-tuning of virulence factors, and has the potential for accelerated genome evolution.
副猪嗜血杆菌是格拉泽氏病的病原体,格拉泽氏病是一种以猪的多关节炎、多浆膜炎和脑膜炎为特征的全身性疾病。尽管众所周知副猪嗜血杆菌血清型5是与该疾病相关的最普遍血清型,但菌株之间的遗传差异直到现在才被发现。来自两个血清型5菌株SH0165和29755的基因组已经可用。在这里,我们展示了第三个副猪嗜血杆菌血清型5菌株——正式的血清型5参考菌株长崎的基因组草图。对这三个副猪嗜血杆菌血清型5菌株的全长预测基因进行的电子基因组消减分析分别检测到长崎、SH0165和29755的95个、127个和95个菌株特异性基因(SSG)。我们发现这三个菌株内的基因组多样性很高,部分原因是存在大量移动元件。此外,对范围从2到16 kb的大片段序列多态性(LSP)的详细分析揭示了毒力相关元件中的LSP,如Toll-IL受体、AcrA多药外排蛋白、ATP结合盒(ABC)转运蛋白、脂多糖合成酶和一种不依赖ATP的三方周质(TRAP)转运蛋白。还计算了全基因组密码子适应指数(CAI),其值与其他知名细菌病原体相似。此外,全基因组SNP分析表明,核苷酸变化在与膜相关的基因中倾向于增加。该分析提供了进一步的证据,表明副猪嗜血杆菌的基因组经历了多次横向基因转移(LGT)以及毒力因子的微调,并且具有加速基因组进化的潜力。